Peptidases localization

Some natural antibiotics contain a siderophore structure, for instance, 5i-albomycin 35, which is produced by Streptomyces subtropicus. The linear tripeptide portion chelates Fe(III) and, thereby, is able to utilize the iron-transport system of a range of microorganisms. Subsequent to uptake, peptidases localized in the cytoplasmic membrane hydrolytically release the toxic thioribosyl moiety. In principle, this property can be used for selective drug delivery. Preliminary studies indicated that substantial modification of the siderophore framework can be tolerated by microbial iron-transport systems. Surprisingly, simple modifications can be made to cephalosporin molecules, which endow them with the ability to interact with microorganism iron-transport mechanisms. Thus, simple incorporation of a catechol moiety, as in 36, endows this molecule with enhanced activity against Pseudomonas aeruginosa when compared... 

Ajami, K., Abbott, C.A., McCaughan, G.W. and Gorrell, M.D. (2004) Dipeptidyl peptidase 9 has two forms, a broad distribution, cytoplasmic localization and DPIV-like peptidase activity. Biochimica et Biophysica Acta, 1679, 18-28. 

Enzymes that act on peptide bonds (i.e., peptidases and proteases) hydrolyze peptide bonds in peptides and proteins. We examine first their classification before outlining their localizations and some physiological roles. 

The isolation and investigation of intracellular tissue peptidases is more difficult than that of extracellular peptidases, and, as a result, less is known about such peptidases. Illustrative examples of peptidases with their intracellular localization are presented in Table 2.3 [7a],... 

Membrane alanyl aminopeptidase (microsomal aminopeptidase, amino-peptidase M, EC 3.4.11.2) and peptidyl-dipeptidase A (angiotensin I converting enzyme, EC 3.4.15.1) located in the vascular endothelium and smooth muscle cell surface modulate the levels of vasoactive peptides [23], One of the roles of membrane-bound enzymes is to switch off the action of peptides in the vicinity of the target or to prevent them from gaining access to a region containing receptors that are activated only by locally released peptides. 

The previous chapter offered a broad overview of peptidases and esterases in terms of their classification, localization, and some physiological roles. Mention was made of the classification of hydrolases based on a characteristic functionality in their catalytic site, namely serine hydrolases, cysteine hydrolases, aspartic hydrolases, and metallopeptidases. What was left for the present chapter, however, is a detailed presentation of their catalytic site and mechanisms. As such, this chapter serves as a logical link between the preceding overview and the following chapters, whose focus is on metabolic reactions. 

As illustrated below, the biotransformation of peptides in complex biological media is often due to contributions of only one or a very few enzymes. Indeed, the two main factors that govern the hydrolysis of a peptide in a given tissue are the cellular localization and level of peptidases (i. e.,... 

ACE is a rather nonspecific peptidase that can cleave C-terminal dipeptides from various peptides (dipeptidyl carboxypeptidase). As kininase 11, it contributes to the inactivation of kinins, such as bradykinin. ACE is also present in blood plasma however, enzyme localized in the luminal side of vascular endothelium is primarily responsible for the formation of angiotensin 11. The lung is rich in ACE, but kidneys, heart, and other organs also contain the enzyme. 

After translocation into the mitosome, the N-terminal presequences of mitosomal proteins are cleaved off, most likely by a peptidase that is homologous to the mitochondrial processing peptidase (MPP). The MPP is a matrix-localized metallopeptidase with a zinc binding motif His-X-X-Glu-His that is conserved in the putative mitosomal processing peptidase reported in G. intestinalis (Dolezal et al. 2005). 

In this protocol, enzyme is prepared from a single kiwi fruit, the fruit of the Chinese gooseberry (.Actinidia chinensis), purchased at a local grocery store. The predominant peptidase of the kiwi fruit is a cysteine peptidase called actinidain. 

Most studies of the local actions of opioids on the intestinal mucosa have utilized muscle-stripped sheets of ileal mucosa with attached submucosa mounted in Ussing flux chambers. Peptidase-resistant enkephalin derivatives such as DPDPE decrease short-circuit current, an electrical measure of active transepithelial ion transport, across isolated mucosal sheets from the guinea pig ileum [46,127,128], rabbit ileum [129-131], mouse jejunum [132], and pig distal jejunum/ileum [133]. This effect, which occurs after the application of opioid agonists to the serosal aspect of epithelial sheets, is due to an increase in electroneutral salt absorption and a decrease in electrogenic chloride secretion [46,132,133], In contrast to enkephalin derivatives, opiate alkaloids have limited effects on active transepithelial transport of ions [69]. Pretreat-... 

Hughey RP, Rankin BB, Elce JS, and Curthoys NP. Specificity of a particulate rat renal peptidase and its localization along with other enzymes of mercapturic acid synthesis. Archives of biochemistry and biophysics 186 211-217,1978. 

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